Glycoluril core molecules for combinatorial libraries

ABSTRACT

The present invention provides novel glycoluril derivatives for use as core molecules in combinatorial chemistry. Core molecules of the present invention can contain from one to six building blocks. Preferred building blocks are substituted amine radicals. Combinatorial libraries containing such core molecules are also provided.

Funds used to support some of the work reported herein were provided bythe National Institutes of Health under Grant No. GM 27932. The UnitedStates government may therefore have certain rights in the disclosedinvention.

TECHNICAL FIELD OF THE INVENTION

The field of this invention is combinatorial chemistry. Moreparticularly, the present invention pertains to novel core moleculesused as supports for construction of a combinatorial library.

BACKGROUND OF THE INVENTION

The synthesis of new core molecules is often undertaken to providedifferent orientations of the attached building blocks, therebyincreasing structural diversity. The properties of the core moleculehave (in several assays) been critical to activity, as libraries madewith the same building blocks and linkages have had very differentactivity levels (Carell et al. Chem. Biol. 1995, 2, 171–183). We havepreviously demonstrated the use of 1, 3, 5, 7-cubanetetracarboxylic acidchloride (Carell et al. Angew. Chem., Int. Ed. Engl. 1994, 33,2059–2061; Eaton et al. Angew. Chem., Int. Ed. Engl. 1992, 31,1421–1436; Bashir-Hashemi, A. Angew. Chem., Int. Ed. Engl. 1993, 32,612–613) and both 9,9-dimethyl-2, 4, 5, 7-xanthenetetracarboxylic acidchloride and tetraisocyanate as cores for combinatorial chemistry(Carell et al. Chem. Biol. 1995, 2, 171–183; Carell et al. Angew. Chem.,Int. Ed. Engl. 1994, 33, 2061–2064; Carell et al. Angew. Chem., Int. Ed.Engl. 1994, 33, 2059–2061; Shipps et al. Bioorg. Med. Chem. 1996, 4,655–657; Pryor et al. Tetrahedron 1998, 54(16), 4107–4124).

The fact that the certain receptors and proteins appear to bind theirligands utilizing small clusters of residues for the majority of thebinding interaction has led to the expectation that small molecules maybe capable of triggering a receptor response. It has been anticipatedthat the generation of detailed knowledge concerning the dimerizationmodes and ligand binding domains of single transmembrane domainreceptors will provide a basis for the design of functional agonists aswell as ligand antagonists. However, the noncontiguous and multiplebinding domains involved in both the protein-protein and ligand-proteininteractions make it difficult to assess the dimerization mode or ligandbinding domains in the absence of three-dimensional structuralinformation. This is especially true considering the size of the typicalendogenous ligands including proteins such as EPO (166 residues) whichthemselves contain noncontiguous binding domains which intereact withboth subunits of the dimerized receptor.

Recently, the successful identification of cyclic polypeptides with thecapacity to mimic the action of EPO was reported, together with detailsof the intricate receptor-ligand and receptor-receptor interactions inthe bound complex (Wrighton et al. Science 1996, 273, 458; Livnah et al.Science 1996, 273, 464). Although these results represent a majorachievement, the size (2 to 20 residues) and nature of ligandsidentified would not seem to be immediately applicable as drugcandidates.

In a recently published PCT application (Rebek et al. WO 95/19359), aprocess for making xanthene or cubane based compounds and proteaseinhibitors is described. More particularly, methods for formingcombinatorial libraries and the libraries produced are provided.According to a preferred aspect of the invention, a plurality of coremolecules, the core molecule being a xanthene or cubane derivative, arereacted with a plurality of different “tool” molecules to form a libraryof molecules having non-naturally occurring molecular diversity. Thelibraries are useful for identifying lead compounds which modulate thefunctional activity of a biological molecule. Protease inhibitors thathave been isolated from the libraries also are disclosed.

Combinatorial chemistry, introduced for polypeptide and oligonucleotidelibraries, has undergone a rapid development and acceptance. It iswidely recognized that this approach, when applied to generatingnon-peptide small molecule diversity, has provided a new paradigm fordrug discovery. Perhaps as a consequence of the extension of the conceptfrom peptide and oligonucleotide synthesis, the majority of applicationshave relied on solid-phase synthesis and methodological advancescontinue to extend common synthetic transformations to polymer-supportedversions (Thompson et al. J. A. Chem. Rev. 1996, 96, 555; Friichtel etal. Angew. Chem., Int. Ed. Engl. 1996, 35, 17; Hermkens et al.Tetrahedron 1996, 52, 4527).

A less frequently used complement to adapting solution-phase chemistryto polymer-supported combinatorial synthesis is the development ofprotocols for solution-phase combinatorial synthesis (Han et al. Proc.Natl. Acad. Sci. U.S.A. 1995, 92, 6419). Preceding the disclosure ofefforts on the the development of a multi-step solution-phase parallelsynthesis of chemical libraries (Cheng et al. J. Am. Chem. Soc. 1996,118, 2567; Boger et al. J. Am. Chem. Soc. 1996, 118, 2109; Cheng et al.Bioorg. Med. Chem. 1996, 4, 727, Tetrahedron Paper and Patent), thesingle-step solution-phase synthesis of combinatorial libraries wasdetailed by at least three groups as follows. Smith and coworkers (Smithet al. Bioorg. Med. Chem. Lett. 1994, 4, 2821), prepared a library ofpotentially 1600 amides by reacting 40 acid chlorides with 40nucleophiles. The library was screened as 80 sample mixtures in a matrixformat, allowing immediate deconvolution.

A similar sub-library format was used by Pirrung and Chen (Pirrung etal. J. Am. Chem. Soc. 1995, 117, 1240; Pirrung et al. Chem. Biol. 1995,2, 621) who prepared a series of carbamate mixtures which were screenedfor acetylcholinesterase inhibitory activity. Prior to these efforts, wehave disclosed the single-step construction of large librariespresenting amino acid derivatives attached to rigid core templates witha reliance on amide or urea bond formation (Carell et al. Angew. Chem.,Int. Ed. Engl. 1994, 33, 2059; Carell et al. Bioorg. Med. Chem. 1996, 4,655; Dunayevskiy et al. Anal. Chem. 1995, 67, 2906; Carell et al. Chem.Biol. 1995, 2, 171). Because of the complexity of the combinatoriallibraries resulting from this approach (approaching 100,000 members), aniterative selection strategy based on structural grouping of thebuilding blocks was devised.

In addition to recent advances in this work, substantial progresstowards using solution-phase multicomponent reactions for generatingcombinatorial mixtures has been disclosed. For example, both Ugi andArmstrong have reported four-component condensations including theincorporation of a modifiable isocyanide in combination with resincapture strategy, to provide useful solution-phase library preparations(Ugi et al. Endeavour 1994, 18, 115; Keating et al. J. Am. Chem. Soc.1996, 118, 2574; Armstrong et al Acc. Chem. Res. 1996, 29, 123).

There remains a need in the art, however, for small molecule librariesof chemical compounds and economical methods for producing suchlibraries for use in protein and receptor targets as described above.Furthermore, what is needed is an economical method for theidentification or deconvolution of these active chemical libraries torapidly determine active components.

BRIEF SUMMARY OF THE INVENTION

In one aspect, the present invention provides a core molecule for use inconstructing a combinatorial library. The core molecule has thestructure I, below:

In Structure I, each R is independently hydrogen or —O—R₁. Each R₁ isindependently hydrogen or —CH₂COOR₂, where R₂ is hydrogen or a C₁–C₉hydrocarbon. Preferably, the hydrocarbon is a C₁–C₆ alkyl, a C₁–C₆alkenyl, a C₁–C₆ alkynyl, a C₆ aryl, or a C₆–C₉ aralkyl. This inventionfurther provides a soluble combinatorial library wherein each librarymember comprises a core molecule of this invention and a building block.In a preferred embodiment, the building block is a substituted amineradical.

BRIEF DESCRIPTION OF THE DRAWINGS

In the drawings that form a portion of the specification,

FIG. 1 shows the synthesis of certain tetrasubstituted glycoluril coremolecules.

FIG. 2 shows the synthesis of certain disubstituted glycoluril coremolecules.

FIG. 3 shows the synthesis of certain disubstituted glycoluril coremolecules.

FIG. 4 shows one way to activate certain disubstituted core molecules.

FIG. 5 shows one embodiment of a core molecule with the invention.

FIG. 6 shows the synthesis of certain heterotetrasubstituted glycolurilcore molecules for use in stepwise library synthesis.

FIG. 7 shows an alternative heterotetrasubstituted glycoluril coremolecules.

FIG. 8 shows novel intermediates used in the synthesis ofselectively-deprotectable heteropolysubstituted glycoluril coremolecules for deconvoluting molecular libraries.

FIG. 9 shows several preferred core molecules of the current invention.

FIG. 10 shows a preferred embodiment for library formation using oneactivated disubstituted glycoluril core molecule.

FIG. 11 shows an intermediate compound of this invention.

DETAILED DESCRIPTION OF THE INVENTION

I. The Invention

The invention provides novel core molecules suitable for use incombinatorial organic chemistry and the use of those core molecules inpreparing and deconvoluting combinatorial libraries. Furthermore, theinvention is directed to deconvolution strategies used to simplifycomplex libraries and build individual molecular species based on thesecores. The core molecules represent an attempt to further exploreshape-space and increase the structural diversity of prepared libraries,as well as to incorporate recognition elements in the cores to increasethe chances for interaction with biological targets.

II Core Molecules

A core molecule of this invention is a derivative of a glycouril and hasthe structure shown below.

R and R₁ represent the putative sites of attachment of library members(e.g., building blocks) to the core molecule. The structure shows sixpossible sites of attachment. In a preferred embodiment, from 2 to 4sites are used at any given time for attachment. Where a given site isnot used for attachment to a library member, a hydrogen replaces R orR₁.

X can be a C₁–C₆ alkyl, C₁–C₆ alkenyl, C₁–C₆ alkynyl, C₆ aryl, or C₆–C₉aralkyl. X can be linear or cyclic and can be unsubstituted orsubstituted at each carbon atom with, for example, a halogen. In apreferred embodiment, X is phenyl. In accordance with this embodiment, acore molecule has the structure below

where R, R₁ and X have the meaning set forth above. R₃ can be hydrogen,a straight or branched C₁–C₆ linear alkyl (unsubstituted or substitutedwith a halogen), or a C₁–C₆ alkoxy. The R₃ group can be joined to any ofthe cyclic carbon atoms that are not linked to R. Each R is thusindependently hydrogen or —O—R₁. R₁ is hydrogen or CH₂COO—R₂, where eachR₂ is independently hydrogen, C₁–C₆ alkyl, C₁–C₆ alkenyl, C₁–C₆ alkynyl,C₆ aryl, or C₆–C₆ aralkyl. R₂ can be linear or cyclic. R₂ can beunsubstituted or substituted at one or more carbon atoms with, forexample, a halogen. A preferred halogen is fluoride (F).

An “alkyl” group refers to a saturated aliphatic hydrocarbon, includingstraight-chain, branched-chain, and cyclic alkyl groups. The alkyl groupmay have 1 to 12 carbons, or may have 3 to 9 carbons. The alkyl groupmay be substituted or unsubstituted. When substituted, the substitutedgroups may be hydroxyl, cyano, halogen, alkoxy, ═O, ═S, NO₂ or N(CH₃)₂,amino, SH, SR′, or aryl where R′ is alkyl ayrl or aralkyl.

An “alkenyl” group refers to an unsaturated hydrocarbon group containingat least one carbon-carbon double bond, including straight-chain,branched-chain, and cyclic groups. The alkenyl group may have 2 to 12carbons, or may have 3 to 9 carbons. The alkenyl group may besubstituted or unsubstituted. When substituted the substituted groupsmay be hydroxyl, cyano, halogen, alkoxy, ═O, ═S, NO₂ or N(CH₃)₂, amino,SH, or SR′, or aryl.

An “alkynyl” group refers to an unsaturated hydrocarbon group containingat least one carbon-carbon triple bond, including straight-chain,branched-chain, and cyclic groups. The alkynyl group may have 2 to 12carbons, or may have 3 to 9 carbons. The alkynyl group may besubstituted or unsubstituted. When substituted the substituted groupsmay be hydroxyl, cyano, halogen, alkoxy, ═O, ═S, NO₂ or N(CH₃)₂, amino,SH, SR′, or aryl.

An “alkoxy” group refers to an “—O-alkyl” group, where “alkyl” isdefined as described above.

An “aryl” group refers to an aromatic group which has at least one ringhaving a conjugated pi electron system and includes carbocyclic aryl,heterocyclic aryl and biaryl groups, all of which may be optionallysubstituted. The substituents of the aryl groups may be hydroxyl, cyano,halogen, alkoxy, alkyl, alkenyl, alkynyl, amino, or aryl groups.

An aralkyl group refers to an alkyl (as described above) covalentlybonded to an aryl group (as described above).

Carbocyclic aryl groups are groups wherein the ring atoms in thearomatic ring are all carbon atoms. The carbon atoms are optionallysubstituted. Carbocyclic aryl groups include monocyclic carbocyclic arylgroups and optionally substituted naphthyl groups.

An “amide” refers to an —C(O)—NR″R′″, where each of R″ and R′″ arealkyl, aryl, aralkyl or hydrogen.

An “ester” refers to an —C(O)—OR′, where R′ may be alkyl, aryl, oraralkyl.

An “amine” refers to a —N(R″)R′″, where R″ and R′″, may be independentlyhydrogen, alkyl, aryl, or aralkyl.

An ether refers to R—O—R, where R is either alkyl, aryl, or aralkyl.

In a preferred embodiment, each R₃ is hydrogen and a compound of thisinvention corresponds to Structure I, below, where R, R₁ and R₂ are thesame as defined above.

While a compound of Structure I can be linked to 6 building blocks, itis preferred that Structure I contain from 2 to 4 building blocks. Those2 to 4 building blocks can be linked to Structure I at any of the 6positions indicated. Thus, preferred compounds corresponding toStructure I are shown below as Structures II, III, IV, V, and VI.Especially preferred core molecules are shown in FIGS. 1, 2, 3, 5, 7 and9.

The present invention further provides combinatorial libraries whereineach of the library members comprises a substituted core molecule as setforth below.

Each core molecule can be linked to from 1 to 6 building blocks. Thebuilding blocks linked to a given core molecule can be the same ordifferent. Preferably, each core molecule is linked to from 2 to 4building blocks. A member of such a library thus has the Structure VII,shown below.

In Structure VII, each R₄ is independently hydrogen or —CH₂COA and eachR₅ is independently hydrogen or —OCH₂COA, where A is a building block.Any building block can be used to construct a library so long as thatbuilding block is reactive with an activated carboxylic acid group. In apreferred embodiment, the building blocks are substituted amineradicals. Primary and secondary amine radicals are preferred. As usedherein, the term “substituted amine radical” means that at least oneatom bound to the amine nitrogen is not hydrogen. Such substituted amineradicals are well known in the art. Exemplary such substituted amineradicals are 2-amino-5-diethylaminopentane,2(2-aminoethyl)-1-methylpyrrolidine, 1-(2-aminoethyl)-Pyrrolidine,4-(2-aminoethyl)morpholine, 2-(2-aminoethyl)-pyridine,1-amino-4-methylpiperazine, 4-amino morpholine, furfurylamine,4-methoxybenylamine, 1-aminopiperidine, 4-(aminoethyl)pyridine, aminoacids or derivatives thereof (e.g., H-Ala-OMe, H-AlaOtBu, H-Asn-OtBu,H-Asp(OMe)-OtBu, H-Asp(OtBu)-OtBu, H-Glu(OtBu).OtBu, HGly-OMe,H-Ile-OMe, H-Ile-OtBu, H-Leu-OtBu, H-Lys(BOC)—OMe, H-Lys(BOC)OtBu,H-Met-OMe, H-Phe-OtBu, H-Pro-OtBu, H-Ser(tBu).OtBu-H-Ser-OMe,HThr(tBu)-OMe, H-Tyr-OMe, H-Val-OMe, H-Val-OtBu, H-Tyr(tBu)-OMe,H-Ser(tBu)OMe), Aniline, Benzylamine, Phenethylamine, 2,2-diphenylethylamine, Isobutylamine, Butylamine, N,N-diethylethylenediamine,3-(dimethylamino)propylamine, Aminomethyl cyclopropane, 4-amino-1-benzylpiperidine, 4-(3-aminopropyl)morpholine,1-(3-aminopropyl)-2-pyrrolidinone, and Ethyl 4-amino-1-piperidinecarboxylate.

Especially preferred amine building blocks are2-amino-5-diethylaminopentane, 2(2-aminoethyl)-1-methylpyrrolidine,1-(2-aminoethyl)-Pyrrolidine, 4-(2-aminoethyl)morpholine,2-(2-aminoethyl)-pyridine, 1-amino-4-methylpiperazine, 4-aminomorpholine, furfurylamine, 4-methoxybenylamine, 1-aminopiperidine,4(aminoethyl)pyridine, Aniline, Benzylamine, Phenethylamine,2,2-diphenyl ethylamine, Isobutylamine, Butylamine,N,N-diethylethylenediamine, 3-(dimethylamino)propylamine, Aminomethylcyclopropane, 4-amino-1-benzyl piperidine, 4-(3-aminopropyl)morpholine,1-(3-aminopropyl)-2-pyrrolidinone, and Ethyl 4-amino-1-piperidinecarboxylate.

A combinatorial library of this invention is useful for rapidlygenerating and developing large numbers of drug candidate molecules. Theinvention is useful for systematically synthesizing a large number ofmolecules that may vary greatly in their chemical structure orcomposition, or that may vary in minor aspects of their chemicalstructure or composition. The invention is also useful for randomlygenerating a large number of drug candidates, and later optimizing thosecandidates that show the most medicinal promise. A soluble combinatoriallibrary of the present invention may be screened by any method wellknown in the art. These methods include, but are not limited to, ELIZAplating, receptor binding, southern, western and northern blotting, andcompetitive binding.

One such method for identifying an agent to be tested for an ability tobind to and potentially modulate a cellular receptor signal transductionpathway is as follows. The method involves exposing at least onecompound from the combinatorial libraries of the present invention to aprotein comprising a functional portion of a cellular receptor for atime sufficient to allow binding of the combinatorial library compoundto the functional portion of the cellular receptor; removing non-boundcompound; and determining the presence of the compound bound to thefunctional portion of the cellular receptor, thereby identifying acompound to be tested for an ability to modulate a cellular receptorsignal transduction pathway.

One method utilizing this approach that may be pursued in the isolationof such receptor-binding molecules would include the attachment of acombinatorial library molecule, or a portion thereof, to a solid matrix,such as agarose or plastic beads, microtiter wells, petri dishes, ormembranes composed of, for example, nylon or nitrocellulose, and thesubsequent incubation of the attached combinatorial library molecule inthe presence of a potential combinatorial library molecule-bindingcompound or compounds. Attachment to said solid support may be direct orby means of a combinatorial-library-compound-specific antibody bounddirectly to the solid support. After incubation, unbound compounds arewashed away, component-bound compounds are recovered. By utilizing thisprocedure, large numbers of types of molecules may be simultaneouslyscreened for receptor-binding activity. A number of libraries based onthis core have been synthesized. HPLC analysis of small librariesindicates clean reactions with approximately statistical productdistributions.

A core molecule of this invention is typically made as an acid (e.g.,diacid or tetraacid) where R₂ of Structures II-VI is hydrogen. A numberof synthetic routes can be used to prepare such acids. By way ofexample, acids can be prepared by saponifying the corresponding ethyl orbenzyl esters. Alternately, acids can be formed via hydrogenolysis ofcorresponding benzyl esters. Preparation of a tetraacid core molecule(Compound 1) using hydrogenolysis is shown in FIG. 1. The tetraacid,Compound 1, was originally synthesized by saponification of thecorresponding tetraethyl ester. However, Compound 1 proved to be sohighly water soluble that separation of the compound from the saltby-products of the reaction was difficult. By replacing the ethyl esterswith benzyl esters (compound 2) and performing a hydrogenolysis insteadof a saponification Compound 1 was accessible cleanly and in highyields.

Armed with the knowledge of the glycoluril tetraacid's remarkable watersolublity, initial syntheses of other analogs with fewer acidsubstituents were originally based on the hydrogenolysis of thecorresponding benzyl esters, as well (See FIGS. 2 and 3). However, thesolubility of the diacid compounds 3 (FIG. 2) and 4 (FIG. 3) was muchlower in the solvent mixture used for the hydrogenolysis (ethylacetate/ethanol) than the tetraacid 1, and yields for this step rangedin both cases from approximately 35–55%, due primarily to problems withproduct recovery. Fortunately, subsequent trials proved that the diacidswere also less soluble in water than the tetraacid, so saponification ofeither the ethyl or benzyl esters was a viable option; yields of thesaponification reactions are routinely greater than 90%. Diacid Compound3 precipitates immediately upon pouring the reaction mixture into 1MHCl, while diacid Compound 4 crystallizes when chilled overnight afterpouring the reaction mixture into 1M HCl. Because the yields of allreaction steps in both syntheses are quite comparable using either ethylor benzyl esters, it is preferred that benzyl esters be used for thesimple reason that stockpiles of intermediates can be used in anysynthesis, while ethyl ester derivatives could not be used in thesynthesis of the glycoluril tetraacid. Otherwise, the ethyl hydantoateis available in one step from commercially available materials, whilethe benzyl hydantoate requires two steps, but the extra step is simple,high-yielding, and can be performed on a 100 g scale quite readily. Adetailed description of the synthesis of core molecules can be foundhereinafter in the Examples.

III Activation of Core Molecules for Library Construction

As is well known in the art, prior to use as core molecules forcombinatorial library synthesis, it is necessary to activate the acidform of the molecule into a form suitable for library member or buildingblock attachment. Historically, activation of core acids as acidchlorides has been a simple, effective way to accomplish this goal. Inthe case of the glycoluril core molecules, however, the presence of theurea functionality precludes activation as acid chlorides.

Fortunately, alternatives to acid chloride activation are numerous, assynthetic chemists have often found the need to synthesize amide bondsunder milder reaction conditions than are required in the synthesis ofacid chlorides. One option is to make use of a coupling reagent todirectly couple the amine building blocks to the polyacid core. Anotheroption is to activate the acids on the core as some functional groupother than as acid chlorides and isolate the activated core for use in asubsequent amidation step. One unusual, but very important, criterionfor the successful reaction in this case is that the finallibrary-forming reaction must only produce by-products that can betotally removed by non-chromatographic methods. Since a wide variety ofbuilding blocks might be used in any given library synthesis, producinga number of compounds with potentially vastly different elutionprofiles, chromatographic techniques would be contraindicated if alllibrary components are to be kept together as a mixture.

A preferred means of activating the core molecules of this invention isesterification. By way of example, diacid Compound 4 can be activated asthe bis(pentafluorophenyl)ester (Compound 5, FIG. 4) by coupling theacids and pentafluorophenyl with EDC and catalytic DMAP in THF (see FIG.4). The resulting active ester reacts readily with a variety of amines,including relatively unreactive anilines. Additionally,pentafluorophenyl can be removed by aqueous extraction during work-up.The glycoluril core is unaffected by the reaction conditions used fordeprotection of t-butyl ester derivatives of amino acids used asbuilding blocks (neat TFA, 12 h). A similar approach can be used toactivate other forms of glycoluril polyacid core molecules (e.g., diacidCompound 3 or tetraacid Compound 1).

Another preferred means of activating the core molecules of thisinvention is by the use of amide coupling reagents to activate the acidsin situ and react them directly with one or more building blocks (e.g.,a substituted amine radical). A number of these coupling reagents arewell known in the art. Some examples are dicyclohexyl carbodiimide(DCC), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide(EDCáMeI), benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphoniumhexafluorophosphate (PyBOP), bromo-tris-pyrrolidino-phosphoniumhexafluorophosphate (PyBroP), and diphenylphosphoryl azide (DPPA). Manyreactions using these coupling reagents work fairly well, but in somecases it is difficult to completely purify the products withoutresorting to chromatography. A preferred coupling reagent is DPPA. Byway of example, diacid Compound 4 can be activated with DPPA and aminebuilding blocks can be introduced directly on the core molecule (seeFIG. 11). A similar approach can be used to activate other forms ofglycoluril polyacid core molecules (e.g., diacid Compound 3 or tetraacidCompound 1).

IV Use in Forming Combinatorial Libraries

Solution phase synthesis has emerged as one method for the generatingcombinatorial libraries. By synthesizing the combinatorial library insolution, the present invention permits library synthesis that is morerapid and efficient than conventional methods, such as solid phasesynthesis. Solid phase synthesis typically yields only a few nanogramsof product. In contrast, the present invention, by synthesizing insolution, yields milligrams and grams of product.

A library is made by reacting a core molecule of this invention havingactivated carboxylic acid groups (e.g., C₆F₅), prepared as describedabove, with one or more building blocks (e.g., a substituted amineradical) under conditions and for a period of time sufficient forformation of the library member. Molecules in the soluble combinatoriallibrary of the present invention may be purified by any of thetechniques well known in the art. These techniques include, but are notlimited to, precipitation, thin layer chromatography, columnchromatography, high pressure liquid chromatography, crystallization,gel electrophoresis, and filtration.

A number a libraries have been synthesized using a core molecule of thisinvention. In particular, libraries using a core molecule according toStructure II and a number of substituted amines (Aniline, Benzylamine,Phenethylamine, 2,2-diphenyl ethylamine, Isobutylamine, Butylamine,N,N-diethylethylenediamine, 3-(dimethylamino)propylamine, Aminomethylcyclopropane, 4-amino-1-benzyl piperidine, 4-(3-aminopropyl)morpholine,1-(3-aminopropyl)-2-pyrrolidinone, and Ethyl 4-amino-1-piperidinecarboxylate) have been made.

The library can be screened to provide some measure of the activity of alibrary while not providing an opportunity to isolate the activecompound(s) directly. A scheme wherein an initial large library isnarrowed to a single active molecule depends initially on the synthesisof smaller sublibraries and in the final stages on active compoundidentification.

In a hypothetical example, assume that a library containing 3760compounds (from the reaction of a mixture of 8 building blocks withglycoluril tetraacid core molecule having 1) is shown to be active ininhibiting the action of an enzyme in solution. In the next stage ofdeconvolution, 8 sublibraries, each of which lacks one of the originaleight building blocks, is synthesized and assayed for activity. Thoselibraries that still demonstrate activity are known to contain therequisite building blocks for a potent inhibitor, while thosesublibraries that are inactive are known to lack necessary buildingblocks. As each library has one fewer building block than the originalactive library, it is thus possible to look at the inactive sublibrariesand read off the identity of each necessary building block. If there ismore than one active compound in the original library, it is possiblethat more than four building blocks will be identified as important;additional sublibraries can then be synthesized to determine the mostimportant of these, which would presumably correspond to those buildingblocks attached to the most potent inhibitor.

Once the most important four or fewer building blocks are identified,the relative geometries of the substituents on the core molecule in theactive inhibitor can be determined by synthesizing the different isomersindividually via the synthetic scheme disclosed and assaying them eachindividually (For related prior art relating to iterative screeningprocesses, see Shipps et al., Proc. Natl. Acad. Sci., 1997, 94,11833–11838; Carell et al Angew. Chem. Int. Ed., 1994, 33, 2061–2064).

In the more specific case where an activity screen is tied to aselection process, such as screening for tight binders by affinitychromatography, active compounds can be isolated from an initial largelibrary. In this case, the identity of the molecule can be partiallydetermined by mass spectrometry of the active compound itself or thebuilding blocks isolated from the hydrolysis of the amide bonds in theactive compound. However, at this point all that is known is thecomposition of the active, not its geometry. Again, synthesis ofdifferent isomers via the disclosed synthetic scheme is required todefinitively assign the correct geometry to the active compound.

A synthetic scheme for diester/diacid 10 is shown in FIG. 6. Thismolecule incorporates different protecting groups into the molecule thatallow orthagonal deprotection under conditions that would not epimerizeaminoacid substituents. The diethyl ester substituted benzil 11 wassaponified to 12 in almost quantitative yield with lithium hydroxide inaqueous THF. Conversion of this diacid to the diacid chloride 13 wasaccomplished using oxalyl chloride in good yield. Esterification with2,2,2-trichloroethanol provided the protected dione 14.

The dione was condensed with benzyl hydantoate 15, available in twosteps from glycine, to yield the differentially-protected glycoluril 9.Deprotection of the trichloroethyl esters was accomplished by treatmentwith zinc and acetic acid to give the diacid 10. Attempts to condensethe free diacid 12 in a glycoluril-forming reaction only met withsuccess when unsubstituted urea was used. In several attempts withbenzyl hydantoate, the cyclization of the hydantoate to give hydantoinproceeded to the exclusion of the desired condensation; it is thoughtthat the poor solubility of diacid 12 in the reaction medium is toblame.

A synthesis of the “reverse” glycoluril 16 (FIG. 7), in which the benzyland trichloroethyl esters are switched relative to compound 9, met withfailure due to similar reasons. The trichloroethyl hydantoate is morelabile to hydantoin formation than the benzyl analog, and glycolurilformation was not competetive in this case. All of the requiredprecursors (trichloroethyl glycine 17 and trichloroethyl hydantoate 18,(FIG. 8) were synthesized, though, and are available for other use.

A selection of substituted glycoluril core molecules that have beenprepared are shown in FIG. 9. Some of these compounds contain fourcarboxylates, while others have only two. Of those with two, 19 containsacids on the R groups coming from the starting dione, and 20, 21, and 22contain esters coming from the starting urea (FIG. 9). It is interestingto note that the electron-donating substituents on the benzil precursorsleading to all compounds except 20 and 21 prevent the formation of thetrans-substituted compounds. In the case of 20 and 21, wherein the Rgroups are unsubstituted phenyls, a small amount of the trans isomer 21was isolated, albeit in much lower yield (yields were 69% and 8%,respectively).

The Examples that follow illustrate preferred embodiments of the presentinvention and are not limiting of the specification and claims in anyway.

EXAMPLE 1 General Methods

All reagents were purchased from Aldrich Chemical Company and were usedwithout further purification except as noted. Amino acid esters, PyBOP,PyBrOP, and HATU were acquired from Novabiochem (San Diego, Calif.).Deuterated solvents were obtained from Cambridge Isotopes Laboratoriesand deuterated chloroform was dried over 4 Å molecular sieves. Citricacid and HCl refer to IN stock solutions. NMR spectra were recorded oneither a Bruker AC-250, a Bruker AM-300, or a Bruker DRX-600; TMS wasused as a reference in chloroform-d proton spectra; otherwise residualsolvent was used as a reference. Either a Finnegan Mat 8200 (forHRMS/EI) or a VG ZABVSE (for HRMS/FAB) mass spectrometer was used toascertain exact masses. FT-IR spectra were obtained on a Perkin ElmerParagon 1000 PC FT-IR Spectrometer. Silica gel chromatography wasperformed with Silica Gel 60 (EM Science or Bodman, 230400 mesh). TLCanalysis was performed using glass-bound Silica Gel 60 (F254) plates.EDC.MeI=1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide.DMAP=N,N-dimethyl-4-aminopyridine.

EXAMPLE 2 Preparation of Glycoluril dibenzyl ester (Compound 3 a, FIG.2)

Dibenzyl 4,4′-bis(carboxymethoxy)benzil (43.82 g, 81.4 mmol) and urea(14.68 g, 244.4 mmol) (NOTE: 2.5 equivalents can also be usedsuccessfully) were dissolved in 400 mL benzene. TFA (20 mL) was addedand the solution was refluxed under a Dean-Stark trap in a nitrogenatmosphere for 16 h. EtOH was added to the cooled solution and the solidprecipitate was isolated by filtration. The solids were purified bystirring overnight in boiling EtOH. The resulting solids were isolatedby filtration and dried in vacuo, yielding a white powder (36.97 g,73%). ¹H-NMR (600 MHz, DMSO-d⁶): δ 7.65 (s, 4H), 7.33–7.38 (m, 10H),6.94 (d, J=8.8 Hz, 4H), 6.65 (d, J=8.8 Hz, 4 H), 5.13 (s, 4H), 4.71 (s,4H). ¹³C-NMR (151 MHz, DMSO-d⁶): δ 168.66, 160.79, 157.24, 135.82,131.30, 128.60, 128.42, 128.34, 128.20, 113.55, 81.60, 65.98, 64.56.Calc'd for [C₃₄H₃₀N₄O₈+Cs⁺]: 755.1118; HRMS (FAB, NBA/CsI) found755.1148. FT-IR (NaCl disc, cm⁻¹): 3229.6, 1760.0, 1721.7, 1682.8,1667.3, 1610.2, 1494.5, 1454.6, 1416.5, 1175.5, 1140.7, 1110.5, 1082.9,1024.5, 955.0, 836.7, 736.1, 696.6. m.p. 213–217° C. (dec.)

EXAMPLE 3 Preparation of Glycoluril diacid (Compound 3 from FIG. 2)

To a stirred suspension of glycoluril dibenzyl ester from Example 2(1.00 g, 1.61 mmol) in 17.5 mL THF was added a solution of LiOH.H₂O(0.16 g, 3.9 mmol) in 3.5 μL water. The resulting mixture was vigorouslystirred at RT for 17 h. The mixture was poured into 90 mL HCl. Theresulting white solids were isolated by filtration and were dried atelevated temperature, yielding the diacid (0.68 g, 96%). ¹H-NMR (600MHz, DMSO-d⁶): δ 7.66 (s, 4H), 6.94 (d, J=8.8 Hz, 4H), 6.62 (d, J=8, 7Hz, 4H), 4.50 (s, 4H). ¹³C-NMR (151 MHz, DMSO-d⁶): δ 160.90, 157.58,130.98, 128.42, 113.55, 81.69, 64.72, 21.09. Calc'd for [C₂₀H₁₈N₄O₈+H+]:443.1203; HRMS (FAB, NBAINal) found 443.1233. FT-IR (DRAK, KBr, cm⁻¹):3381, 3221 (br., v.s.), 2361, 1726, 1684, 1610, 1513, 1476, 1445, 1419,1302, 1235, 1185, 1110, 1074, 954, 839, 780, 737, 634. m.p. 287° C.(dec.)

EXAMPLE 4 Preparation of Glycoluril diacid (Compound 4 from FIG. 3):

A solution of LiOH.H₂O (0.101 g, 2.40 mmol) in 21 mL water was added toa stirred suspension of glycoluril dibenzyl ester from Example 2 (0.590g, 1.00 mmol) in 10 mL THF. This mixture was stirred at RT for 16 h,then was poured into 50 mL HCl. The resulting solution was chilled in arefrigerator. Clear crystals grew in the solution, which were isolatedby filtration and were dried at elevated temperature, yielding thediacid (0.37 g, 90%). ¹H-NMR (600 MHz, DMSO-d⁶): δ 12.62 (br. S, 2H{integrated low}), 8.21 (s, 2H), 7.07 (s, 10H), 3.90 (d, J=17.6 Hz, 2H),3.62 (d, J=17.6 Hz, 2H). ¹³C-NMR (151 MHz, DMSO-d⁶): δ 171.06, 159.54,137.87, 133.96, 128.79, 128.38, 128.35, 128.19, 127.62, 127.51, 88.64,79.90, 43.08. Calc'd for [C₂₀H₁₈N₄O₆+H⁺]: 411.1305; HRMS (FAB, NBA/NaI)found 411.1317. FT-IR (DRAK, KBr, cm⁻¹): 3456.6, 3228.0 (br.), 1734.8,1700.2, 1474.6, 1449.8, 1399.8, 1340.7, 1225.6, 1147.2, 985.8, 963.9,944.5, 780.7, 703.7, 667.9. m.p. 255° C. (dec.)

EXAMPLE 5 Preparation of Glycoluril bis(pentafluorophenyl ester(Compound 5 from FIG. 4)

To a stirred suspension of glycoluril diacid 4 from Example 4 (1.00 g,2.44 mmol) in 100 mL THF was added pentafluorophenyl (1.80 g, 9.76mmol), EDC.MeI (3.12 g, 10.5 mmol) and catalytic DMAP. The mixture wasstirred at RT for 14 h. The solvent was removed by rotary evaporationand the resulting paste was sonicated in EtOAc and filtered to removeinsoluble material. The filtrate was run through a plug of silica gelwith EtOAc. The filtrate was concentrated and sonicated in Et₂O toremove pentafluorophenyl. The white powder was isolated by filtration,rinsed with Et₂O and dried in vacuo, yielding the diester (1.42 g, 79%).¹H-NMR (600 MHz, DMSO-d⁶): δ 8.58 (s, 2H), 7.15–7.03 (m, 10H), 4.77 (d,J=18.4 Hz, 2H), 4.38 (d, J=18.4 Hz, 2H). ¹³C-NMR (151 MHz, DMSO-d⁶): δ166.77, 159.03, 141.52 (m), 139.83 (m), 138.54 (m), 137.06, 136.89 (m),133.31, 129.08, 128.55, 127.79, 127.69, 127.31, 88.34, 80.48, 42.39.¹⁹F-NMR (565 MHz, DMSO-d⁶): δ-152.61 (d, J=24 Hz), −157.44 (t, J=24 Hz),−162.16 (t, J=24 Hz). Calc'd for [C₃₂H₁₆F₁₀N₄O₆+Cs⁺]: 874.9964; HRMS(FAB, NBA/CsI) found 875.0004. FT-IR (NaCl disc, cm⁻¹): 1788.7, 1714.4,1521.7, 1450.0, 1103.7, 998.1.

EXAMPLE 6 Preparation of Glycoluril bis(leucine t-butyl ester) adduct(Compound 6 from FIG. 10)

A. Reaction of bis(pentafluorophenyl ester). To a solution of leucinet-butyl ester hydrochloride (34.8 mg, 0.155 mmol) in 1 mL DMF and 0.5 mLEt₃N chilled in an ice bath was added a partial solution/suspension ofglycoluril bis(pentafluorophenyl ester) Compound 5 (50.4 mg, 0.0683mmol) in 3.5 mL CH₂Cl₂. The solution warmed over 2.5 h, then was dilutedwith CH₂Cl₂ and was washed with water (3×) and brine (3×). The organicphase was dried over MgSO₄, was filtered, and was concentrated by rotaryevaporation to pale yellow solids which were dried in vacuo (53 mg,quant.)

B. Reaction of diacid with DPPA. A stirred solution of glycoluril diacidCompound 4 (200 mg, 0.487 mmol) and of leucine t-butyl esterhydrochloride (240 mg, 1.07 mmol) in 2 mL DMF was chilled in a salt/icebath. To this solution was added diphenylphosphoryl azide (231 μL, 294mg, 1.07 mmol) and Et₃N, (298 μL, 217 mg, 2.14 mmol) and the solutionwas stirred 17 h, warming to RT. The solvent was removed by rotaryevaporation and the residue was taken up in EtOAc and was washed withwater (2×) and brine (3×). The organic phase was dried over MgSO₄, wasfiltered, and was concentrated by rotary evaporation to an off-whitefoam (323 mg, 88%). ¹HNMR (600 MHz, CDCl₃): δ 7.24–7.21 (m, 2H),7.16–6.97 (m, 10H), 6.85 (br. s, 1H), 6.78 (br. s, 1H), 4.41–4.37 (m,2H), 3.95 (d, J=16.3 Hz, 1H), 3.82 (s, 2H), 3.65 (d, J=16.5 Hz, 1H),1.70–1.46 (m, 6H), 1.44 (s, 9H), 1.42 (s, 9H), 0.95 (d, J=6.6 Hz, 3 H),0.93 (d, J=6.5 Hz, 3H), 0.93 (d, J=6.4 Hz, 3H), 0.88 (d, J=6.4 Hz,3H).). ¹³CNMR (151 MHz, CDCl₃): δ 172.57, 172.41, 168.57, 168.52,160.98, 160.59, 136.57, 131.90, 129.51, 129.38, 129.00, 128.82, 1283.63,128.27, 127.57, 123.48, 120.50, 120.47, 90.79, 82.10, 82.02, 80.69,51.93, 51.75, 45.96, 45.79, 41.46, 41.33, 28.08, 28.06, 25.00, 24.98,22.83, 22.74, 22.33, 22.21. Calc'd for [C₄₀H₅₆N₆O₈+Na⁺]: 771; LRMS (FAB,NBA/NaI) found 771. FT-IR (NaCl disc, cm⁻¹): 3242.3, 2958.7, 1701.9,1458.4, 1150.0.

EXAMPLE 7 Preparation of Glycoluril bis(leucine) adduct (Compound 7,FIG. 10)

Glycoluril bis(leucine t-butyl ester adduct) Compound 6 (45 mg, 0.060mmol) was stirred in 5 mL TFA for 15 h. The TFA was removed by rotaryevaporation and the resulting oil was sonicated in 1:1 Et₂O:hexane. Theresulting precipitate was isolated by filtration and was rinsed withEt₂O, yielding a white powder (34 mg, 86%). ¹H-NMR (600 MHz, DMSO-d⁶): δ8.27 (s, 1H), 8.25 (s, 1H), 7.96 (d, J=7.9 Hz, 1H), 7.79 (d, J=7.8 Hz,1H), 7.09–7.02 (m, 10H), 4.28–4.26 (m, 2H), 3.85 (d, J=16.6 Hz, 1H),3.66 (d, J=16.8 Hz, 1H), 3.53 (d, J=16.7 Hz, 1H), 3.52 (d, J=16.8 Hz,1H), 1.79–1.70 (m, 1H), 1.70–1.62 (m, 1H), 1.55–1.48 (m, 4H), 0.92–0.85(m, 12H). ¹³C-NMR (151 MHz, DMSO-d⁶): δ 174.42, 174.19, 168.47, 168.39,159.73, 159.69, 137.62, 133.37, 128.72, 128.26, 127.49, 127.36, 89.12,79.61, 50.30, 45.77, 44.22, 44.05, 40.28, 24.21, 22.85, 22.79, 21.41,8.58. Calc'd for [C₃₂H₄₀N₆O₈+Cs⁺]: 769; LRMS (FAB, NBA/CsI) found 769.

EXAMPLE 8 Preparation of Glycoluril tetrakis(pentafluorophenyl ester)

A solution of glycoluril tetraacid (200 mg, 0.358 mmol),pentafluoro-phenyl (527 mg, 2.86 mmol), EDC-MeI (847 mg, 2.85 mmol), andcatalytic DMAP in 20 mL THF was stirred at RT for 8 h. The solvent wasremoved by rotary evaporation and the residue was taken up in EtOAc andshaken. Insoluble material was removed by filtration and the filtratewas concentrated and purified by silica gel chromatography (100% EtOAc).Product-containing fractions were combined and concentrated by rotaryevaporation. Excess pentafluorophenyl co-eluted with the product and wasremoved by sonicating the resulting oil in Et₂O. White solids wereisolated by filtration and were dried in vacuo (62 mg, 15%). ¹H-NMR (600MHz, DMSO-d⁶): δ 8.53 (s, 2H), 6.99 (d, J=8.8 Hz, 2H), 6.98 (d, J=8.7Hz, 2H), 6.76 (d, J=8.3 Hz, 4H), 5.22 (s, 2H), 5.21 (s, 2H), 4.77 (d,J=18.3 Hz, 2H), 4.37 (d, J=18.3 Hz, 2H). Calc'd for [C₄₈H₁₈F₂₀N₄O₁₂+H+]:1223.0680; HRMS (FAB, NBA/CsI) found 1223.0609.

1. A compound of the structure I, below

where each R is independently hydrogen or —OR₁, each R₁ is independentlyhydrogen or CH₂COOR₂ and each R₂ is independently hydrogen, C₁–C₆ alkyl,C₁–C₆ alkenyl, C₁–C₆ alkynyl, C₆ aryl, or C₆–C₉ aralkyl, with theproviso that at least R₁ be CH₂COOR₂.
 2. The compound of claim 1 whereineach R is hydrogen.
 3. The compound of claim 1 wherein each R is OR₁. 4.The compound of claim 1 wherein two of the R₁ groups are hydrogen. 5.The compound of claim 1 wherein each R is OR, and two of the R₁ groupsare hydrogen.
 6. The compound of claim 1 wherein R₂ is a C₆ aryl.
 7. Thecompound of claim 6 wherein the C₆ aryl is a halo-substituted C₆ aryl.8. The compound of claim 7 wherein the halo-substituted C₆ aryl is C₆F₅.9. The compound of claim 1 wherein R₂ is a C₂ alkyl.
 10. The compound ofclaim 9 wherein the C₂ alkyl is ethyl.
 11. The compound of claim 9wherein the C₂ alkyl is halo-substituted C₂ alkyl.
 12. The compound ofclaim 11 wherein the halo-substituted C₂ alkyl is 2,2,2-trichloroethyl.13. The compound of claim 1 wherein R₂ is a C₇ aralkyl.
 14. The compoundof claim 13 wherein the C₇ aralkyl is benzyl.
 15. The compound of claim1 having the structure